Related gene-specific medical variations for Gene (Select 390212) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282258	NM_206997.1(GPR152):c.191C>T (p.Thr64Met)	CABP4, GPR152 (T64M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533206	NM_206997.1(GPR152):c.266T>C (p.Leu89Pro)	CABP4, GPR152 (L89P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519515	NM_206997.1(GPR152):c.180T>A (p.His60Gln)	CABP4, GPR152 (H60Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2480630	NM_206997.1(GPR152):c.161C>T (p.Ala54Val)	CABP4, GPR152 (A54V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407519	NM_206997.1(GPR152):c.57G>C (p.Glu19Asp)	CABP4, GPR152 (E19D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357316	NM_206997.1(GPR152):c.193C>T (p.Arg65Cys)	CABP4, GPR152 (R65C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 802691	NC_000011.10:g.67452544C>T	CABP4, GPR152 (G61R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign

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